Field of the Invention
[0001] This invention relates to a gas flow indicator. Particularly, but not exclusively,
the invention relates to a gas flow indicator for use in medical equipment such as
that employed in respiratory care and airway management (for example, in equipment
used for the delivery of gases to and from a patient).
Background to the Invention
[0002] There are many instances when it is desirable to monitor a patient's breathing and/or
the gases they are inhaling or exhaling. For example, a patient may be administered
with a general anaesthetic prior to a surgical procedure. In this case, the anaesthetic
may be provided in the form of a gas which is delivered to the patient through a mask
or tube inserted via the patient's mouth or nose and into their trachea. In some cases,
patients are anaesthetised in an anaesthetic room before being transferred to a separate
surgical theatre and so it is necessary for the patient to be disconnected from the
anaesthetic equipment in the anaesthetic room and reconnected to the anaesthetic equipment
in the theatre.
[0003] Disposable heat moisture exchangers (HME's) are commonly used to warm and humidify
otherwise cold gases before they pass into a patient's lungs. Thus, effectively, an
HME serves as an artificial nose in circumstances where gases are being delivered
to a patient through tubes or masks which are arranged to bypass the nose. Typically,
an HME will include a gas inlet for connection to a gas supply, a gas outlet for connection
to an endotracheal tube or laryngeal mask, and a filter therebetween. The filter serves
to trap heat and moisture exhaled from the patient's lungs and enables incoming gases
to return this heat and moisture to the patient's lungs on inhalation. HME's typically
also include a sampling port through which an anaesthetist can monitor the concentration
and flow rate of the gases being supplied to the patient. For example, they may monitor
the amount of oxygen and/or anaesthetic being delivered to the patient. Usually, the
gases will be monitored through the sampling port when the patent is in the anaesthetic
room and then the monitoring equipment will be disconnected from the sampling port
to allow the patent to be transferred to the theatre. Once in theatre, the sampling
port may be reconnected to further monitoring equipment or it may simply be closed
off by a cap. However, it is not uncommon for an anaesthetist to forget to reconnect
or close the sampling port, causing gases to escape from the open sampling port so
that the patient is not effectively ventilated.
[0004] It is also common to use a disposable oxygen enrichment device to provide a patient
with a higher than normal concentration (e.g. 50%) of oxygen in the air that they
breath, when transferring the patient from theatre to a post-operative recovery room.
Such a device is usually connected to a portable oxygen cylinder and typically comprises
a reservoir configured to receive oxygen flowing from the cylinder through a first
inlet, a second inlet which is open to the air and an outlet arranged to provide a
mixture of air and oxygen from the reservoir to the patient through a suitable tube
or mask. The reservoir is sometimes configured as a rigid component that is shaped
like a cigar or it may be constituted by a flexible bag such as in patent application
PCT/AU96/00417. An advantage of using a flexible bag as the reservoir is that the bag will deflate
and inflate to provide a visible indication that the patient is breathing (i.e. inhaling
and exhaling). However, if the oxygen cylinder is empty, disconnected or delivering
oxygen at an incorrect flow rate, the patient may still be breathing regularly (and
the bag inflating and deflating accordingly) but they will not be receiving the required
level of oxygen. Moreover, they may, in fact, be re-breathing their own expressed
air which is highly undesirable since it results in the patient obtaining progressively
decreasing concentrations of oxygen and progressively increasing concentrations of
carbon dioxide.
[0005] US2003/0041859 discloses a mouthpiece adapter and patient feedback for an inhaler. There is a described
a mouthpiece adapter for an inhaler which comprises a connecting side for connecting
to a mouthpiece of an inhaler and a mouth piece side of reduced size relative to the
inhaler mouthpiece and a transition section between the connecting side and the mouthpiece
side. This enables young children, for example, to use inhalation chambers mask free
and aims to solve the issue of consistent patient inhalation in physically challenged
patients.
[0006] US2008/0087287 describes a mask system configured for use in a clinical or hospital environment
where one or more components of the mask system are configured to promote single patient
use. There is further described a valve member 34 configured to provide an audible
indication, for example, a whistle which provides comfort or positive feedback to
the patient or clinician that the device is assembled properly and that pressurised
gas is being properly channeled.
It is therefore an aim of the present invention to provide a gas flow indicator that
addresses the above-mentioned problems.
[0007] According to the present invention there is provided a breathing mask as defined
in claim 1.
[0008] Embodiments of the present invention therefore provide a simple and effective mechanism
for quickly detecting if gas is flowing as it should through a breathing mask. Importantly,
any person monitoring the gas flow need not look at the gas flow indicator in order
to know whether or not the gas is flowing as it should. Instead, those people may
be busy with other tasks, safe in the knowledge that they will be alerted to any potential
problems by an audible sound (or lack thereof). Moreover, the audible sound generated
by the gas flow indicator will enable a listener to quickly detect the location of
a potential problem by following the sound to its source.
[0009] The gas flow indictor may be arranged to indicate correct gas flow to a patient or
it may be arranged to indicate incorrect gas flow - for example, when gas is escaping
and not reaching the patient. Thus, depending on the arrangement of the gas flow indicator,
the presence of an audible sound may signal correct gas flow and the absence of an
audible sound may signal incorrect gas flow (e.g. to indicate that the patient is
not breathing). Alternatively, the absence of an audible sound may signal correct
gas flow and the presence of an audible sound may signal incorrect gas flow (e.g.
to indicate that gas is escaping).
[0010] The medical equipment may be configured for respiratory care and/or airway management.
[0011] In embodiments of the present invention, the gas flow indicator may be provided in
medical equipment disposed close to a patient's air inlet so as to indicate if there
is a problem with the gases getting to the patient.
[0012] The gas flow indicator may be disposable. The gas flow indicator may be configured
for retro-fitting to existing medical equipment. Alternatively, the gas flow indicator
may integrally be formed with the medical equipment. The audible indication may be
provided by a whistling means. The whistling means may comprise an occlusion arranged
to force gas through a narrow opening to create an audible sound. Alternatively, the
whistling means may comprise a blade configured to bisect a flow of gas, thereby creating
a turbulent vortex which causes the gas to vibrate to make an audible sound. The whistling
means may further comprise a chamber in which the gas may resonate. The chamber may
be configured such that the gas resonates therein at a pre-determined frequency. The
whistling means may further comprise a ball or other structure arranged to rattle
in the gas flow.
The gas flow indicator may be configured to maintain an audible indication of gas
flow at all times when the breathing mask is in use. Accordingly, the gas flow indicator
will serve as an additional safety feature to reassure listeners that gas is flowing
through the medical equipment as intended. Of course, in this instance, the absence
of the audible indication at any point during use will denote that gas is not flowing
as intended.
In other embodiments, the medical equipment may be constituted by an oxygen enrichment
device. The oxygen enrichment device may comprise a reservoir configured to receive
oxygen flowing from an oxygen cylinder through a first inlet, a second inlet which
is open to the air and an outlet arranged to provide a mixture of air from the second
inlet and oxygen from the reservoir to the patient through a suitable tube or mask.
The reservoir may be configured as a rigid (e.g. cigar-shaped) component or a flexible
component, such as a bag. The gas flow indicator may be located in the first inlet
and may be arranged to provide an audible indication when gas is correctly flowing
from the cylinder into the reservoir.
[0013] Accordingly, the lack of an audible sound will indicate that there is a problem with
the oxygen supply. For example, the cylinder may be empty (which happens quite often
since relatively small cylinders are employed to make them easily portable), or the
cylinder may not have been set correctly (e.g. the gas supply may be turned off or
not set to deliver the desired flow rate). In each of the above cases, the result
is that not enough oxygen is flowing into the reservoir for inhalation by the patient.
As a consequence, the patient will be breathing in a hypoxic mixture not containing
sufficient oxygen. Moreover, the patient may be re-breathing their own expressed air
containing progressively decreasing concentrations of oxygen and progressively increasing
concentrations of carbon dioxide. Thus, the gas flow indicator in this embodiment
can quickly alert staff to the fact there is a problem with the oxygen supply even
if the bag is inflating and deflating, as expected.
[0014] In certain embodiments, the gas flow indicator may be configured only to provide
an audible sound when gas is flowing at a pre-determined flow rate. For example, it
may desirable to provide a patient with a 50% mixture of air and oxygen, and this
might be achievable with an oxygen supply set to provide 3 litres per minute. Thus,
the gas flow indicator may only provide an audible sound when gas is flowing at 3
litres per minute. This would therefore help staff to determine that the correct flow
rate had been selected. It might also help to ensure that gas is not wasted by employing
a higher than necessary flow rate. Consequently, running costs could be reduced.
[0015] In particular embodiments, the first inlet may pass orthogonally through the second
inlet. In which case, the gas flow indicator may be located in the path of gas flowing
through the first inlet and in the path of gas flowing through the second inlet. Accordingly,
the inhalation and/or exhalation of a patient's breath may affect (e.g. interrupt
or slow) the audible sound produced by the gas flow indicator so that it may also
be possible to detect a patient's breathing by the variation of the audible sound.
[0016] According to the present invention the medical equipment is constituted by a breathing
mask. The breathing mask may be of the type commonly used for patients in recovery
wards. The breathing mask is configured for supplying air/oxygen provided through
at least one inlet to a patient. The gas flow indicator is provided in the at least
one inlet and is arranged to provide an audible indication when gas is correctly flowing
into the mask (i.e. when the patient is inhaling). Alternatively or additionally,
the gas flow indicator may be configured to provide an audible indication when gas
is correctly flowing out of the mask (i.e. when the patient is exhaling). Thus, in
embodiments of the invention, the gas flow indicator may generate a rhythmical sound
in response to a patient's breathing. In this instance, it is envisaged that the gas
flow indicator may be selectively coupled to a standard breathing mask when required.
Alternatively, the staff on each ward may have access to one supply of masks without
gas flow indicators and another supply of masks including gas flow indicators so that
they can select which type of mask to use with any given patient. In either case,
the staff may choose to use a mask with a gas flow indicator only when they deem it
necessary to monitor a particular patient's breathing. This is advantageous since
it may be difficult to identify an individual patient having problems breathing if
a number of people on the same ward are all provided with masks generating noises
associated with their breathing.
Brief Description of the Drawings
[0017] Specific embodiments of the various aspects of the present invention are described
in more detail below in relation to the accompanying drawings, in which:
Figure 1 illustrates an arrangement in which a gas flow indicator is incorporated
into an HME;
Figure 2A shows an enlarged cross-sectional view of the sampling port of the HME of
Figure 1, showing the whistling means therein;
Figure 2B shows an enlarged cross-sectional view of the sampling port of the HME of
Figure 1, having an alternative whistling means therein;
Figure 3A shows an enlarged cross-sectional view of the whistling means illustrated
in Figure 2A but configured as a discrete gas flow indicator;
Figure 3B shows an enlarged cross-sectional view of an alternative whistling means
configured as a discrete gas flow indicator;
Figure 4 shows an arrangement in which a gas flow indicator is incorporated into a
rigid oxygen enrichment device;
Figure 5 shows an arrangement in which a gas flow indicator is incorporated into a
flexible oxygen enrichment device;
Figure 6 shows an enlarged part cross-sectional view of an inlet of the flexible oxygen
enrichment device of Figure 5, illustrating the whistling means therein; and
Figure 7 shows an embodiment of the present invention in which a gas flow indicator
is incorporated into a breathing mask.
Detailed Description of Certain Embodiments
[0018] With reference to Figure 1, there is illustrated a heat moisture exchanger (HME)
10 comprising a gas flow indicator 12. The heat moisture exchanger 10 comprises a
cylindrical inlet 14 for connection to a gas supply, a cylindrical outlet 16 for connection
to an endotracheal tube or laryngeal mask, and a filter 18 therebetween. The filter
18 is configured to trap heat and moisture on exhalation and to return heat and moisture
on inhalation.
[0019] A cylindrical sampling port 20 is provided adjacent the inlet 14 and, in this instance,
the gas flow indicator 12 is housed within the sampling port 20 and is configured
to provide an audible indication when gas is exiting the HME 10 through the sampling
port 20 and into the atmosphere.
[0020] It will be understood that the HME 10 is configured as a single use disposable item
to avoid the need for sterilisation between subsequent uses.
[0021] In use, the inlet 14 is connected to an anaesthetic machine for the delivery of anaesthetic
gas to a patient and the outlet 16 is connected to an endotracheal tube or laryngeal
mask fitted on the patient. The sampling port 20 may be connected to monitoring equipment
or may be closed by a cap when not required. However, if nothing is connected to a
free end 22 of the sampling port 20 (i.e. it is not connected to further equipment
or close off by a cap), gas entering the HME10 will escape into the atmosphere and
this will cause the gas flow indicator 12 to generate an audible sound, thereby alerting
persons close by that there is a problem. Accordingly, the gas flow indicator 12 will
serve as a safety mechanism to alert personnel that gas (in this case, anaesthetic
gas) is escaping and therefore the patient may not be receiving gases as intended.
[0022] Figure 2A shows the structure of the gas flow indictor 12 in situ within the sampling
port 20. Thus, it can be seen that the gas flow indicator 12 comprises a whistling
means provided by a first transverse baffle 24 and a second transverse baffle 26,
spaced from the first baffle 24 and closer to the free end 22 of the sampling port
20 than the first baffle 24. The first baffle 24 has a first aperture 28 disposed
centrally therethrough and the second baffle 26 has a second aperture 30 disposed
centrally therethrough. In this embodiment, the first and second apertures 28, 30
are constituted by circular holes of the same diameter. However, in other embodiments
the first and second apertures 28, 30 may be constituted by holes of other shapes
and each may comprise different dimensions.
[0023] It will be understood that, in use, gas flowing through the sampling port 20 towards
the free end 22 will be forced through the narrow apertures 28, 30 in the baffles
24, 26 before being allowed to exit through the free end 22 and this flow of gas will
therefore produce an audible whistling sound. However, if the free end 22 is closed
by a cap there will be no flow of gas through the sampling port 20 (i.e. the gas will
be relatively static within the sampling port 20) and so no sound will be generated.
Similarly, when the free end 22 is connected to further equipment, the gas flowing
through the sampling port 20 will be reduced to a very low flow rate thereby either
limiting or preventing an audible sound from being generated.
[0024] Figure 2B shows an alternative gas flow indicator 32 that may be situated within
the sampling port 20. The gas flow indicator 32 comprises an occlusion 34 in the form
of a generally cylindrical solid plug which is configured to mate with an inner surface
of the sampling port 20 along a base and substantially around side portions of the
sampling port 20 but which has a cut-out along a top surface to allow gases to flow
along a narrow passageway between the top 36 of the occlusion 34 and the sampling
port 20. A deflector 38 is provided between the occlusion 34 and the free end 22 to
deflect gases flowing over the top 36 of the occlusion 34 back towards the occlusion
and through a narrow gap 39 between the occlusion 34 and the deflector 38. The deflector
38 comprises a first portion 40 angled upwardly towards the free end 22 of the sampling
port 20, the upper end of which is in contact with the top surface of the sampling
port 20 and the lower end of which is disposed at a height slightly below the top
36 of the occlusion 34, and a horizontal portion 42 which extends from the lower end
of the first portion 40 and which terminates close to the occlusion 34 to provide
the narrow gap 39 therebetween.
[0025] In use, the gas flow indicator 32 will generate an audible whistling sound when gas
is forced to flow through the narrow gap 39 before exiting the sampling port 20.
[0026] In the arrangements shown in Figures 2A and 2B, it will be clear that the gas flow
indicators 12 and 32 are integrally formed within the sampling port 20. However, in
other embodiments, the gas flow indicators 12 and 32 may be formed as discrete components
for insertion into a device such as an HME.
[0027] One such discrete gas flow indicator 50 is shown in Figure 3A and comprises a cylindrical
body 52 having a first end 54 and a second end 56, the body 52 housing the whistling
means described above in relation to Figure 2A. Thus, the gas flow indicator 50 comprises
a first transverse baffle 58 and a second transverse baffle 60, spaced from the first
baffle 58 and closer to the second end 56 than the first baffle 58. The first baffle
58 has a first aperture 62 disposed centrally therethrough and the second baffle 60
has a second aperture 64 disposed centrally therethrough. As described previously,
the first and second apertures 62, 64 are constituted by circular holes of the same
diameter. However, in other embodiments the first and second apertures 62, 64 may
be constituted by holes of other shapes and each may comprise different dimensions.
As per the gas flow indicator 12, in use, gas flowing through the body 52 towards
the second end 56 will be forced through the narrow apertures 62, 64 before being
allowed to exit through the second end 56 and this flow of gas will produce an audible
whistling sound.
[0028] Figure 3B shows an alternative discrete gas flow indicator 70 comprising a whistling
means similar to that described above in relation to Figure 2A but wherein the occlusion
is now constituted by a thin aerofoil 72 shaped to smoothly deflect gases upwardly
and through a narrow passageway 74. In this case, the upper end of the curved aerofoil
72 is vertically spaced from a free end 76 of a deflector 78 so as form a vertical
narrow gap 80 therebetween. The deflector 78 is similar to that described above although
in this case the first portion 82 is substantially concave rather than sloped upwardly.
As above, the whistling means is housed in a cylindrical body 84 having a first end
86 and a second end 88. In use, gas may flow in through the first end 86, be deflected
upwardly by the aerofoil 72 through the passageway 74 and towards the deflector 78
where it is then reflected by the first portion 82 and forced backwards and through
the narrow gap 80. The gas will then be reflected once more by the smooth under-surface
of the aerofoil 72 in order to exit through the second end 88. As above, the gas flow
indicator 70 will generate an audible whistling sound when the gas is forced to flow
through the narrow gap 80 before exiting the second end 88.
[0029] Figure 4 shows an arrangement in which a gas flow indicator 90 is incorporated into
a rigid oxygen enrichment device 92. The oxygen enrichment device 92 comprises a generally
cigar-shaped reservoir 94 configured to receive oxygen flowing from an oxygen cylinder
through a first inlet 96, a second inlet 98 which is open to the air and a patient
outlet 100 which connects to a patient via a suitable tube or mask and which is arranged
to provide a mixture of air and oxygen to the patient through the tube or mask. The
reservoir 94 has an open end 101 , opposite to the first inlet 96, which allows excess
gas to flow out of the device 92. On inspiration, the first part of the breath will
mainly comprise oxygen from within the reservoir 94 and the second part of the breath
will mainly comprise air from the open end 101 and the second inlet 98.
[0030] The gas flow indicator 90 is located in path of the first inlet 96 although it is
actually disposed in an extension 102 to the first inlet 96 which is provided within
the body of the reservoir 92. In this embodiment, the gas flow indicator 90 comprises
the whistling mechanism described above in relation to Figure 2A. Accordingly, the
gas flow indicator 90 is arranged to provide an audible indication when oxygen is
correctly flowing from the cylinder into the reservoir 94. As such, the lack of an
audible sound will indicate that there is a problem with the oxygen supply and consequently
the patient may not be receiving the gases intended. This may be caused by the cylinder
being empty or the cylinder may not have been turned on. The lack of sound can therefore
be used to alert personnel to check the status of the oxygen supply.
[0031] In addition to the above, the gas flow indicator 90 is configured only to provide
an audible sound when gas is flowing at a pre-determined flow rate so as to provide
a patient with a 50% mixture of air and oxygen. Accordingly, the lack of an audible
sound may also indicate that the correct flow rate has not been achieved. This is
can be useful in minimising waste and thereby saving costs by ensuring that a higher
than required flow rate is not inadvertently employed.
[0032] Figure 5 shows an arrangement in which a gas flow indicator 1 10 is incorporated
into an oxygen enrichment device 1 12 which is similar to that shown in Figure 4 but
wherein the reservoir is constituted by a flexible bag 1 14. The oxygen enrichment
device 1 12 therefore comprises an elongate bag reservoir 1 14 configured to receive
oxygen flowing from an oxygen cylinder through a first inlet 1 16, a second inlet
1 1 8 which is open to the air and an outlet 120 arranged to provide a mixture of
air from the second inlet 118 and oxygen from the reservoir 1 14 to a patient through
a suitable tube or mask.
[0033] As shown in Figure 6, the gas flow indicator 1 10 is located in path of the first
inlet 116 before the path of the first inlet 116 crosses the path between the second
inlet 118 and the outlet 120. In other embodiments, the gas flow indicator 110 may
be located in the path of gas flowing through the first inlet 116 and in the path
of gas flowing through the second inlet 120 so that the inhalation and/or exhalation
of a patient's breath can interrupt the audible sound produced by the gas flow indicator
1 10 thereby making it possible to detect a patient's breathing by the variation of
the audible sound.
[0034] In the particular embodiment shown in Figure 6, the gas flow indicator 1 10 comprises
the whistling mechanism similar to that described above in relation to Figure 2A although,
in this case, the first baffle 122 has a greater thickness than the second baffle
124. First and second apertures 126 are still provided through each respective baffle
122, 126 to generate an audible indication when oxygen is correctly flowing from the
cylinder into the reservoir 1 14. Thus, as above, the lack of an audible sound will
indicate that there is a problem with the oxygen supply and that the patient may not
be receiving the gases intended.
[0035] Figure 7 shows an embodiment of the present invention in which a gas flow indicator
130, comprising a whistling mechanism as described above in relation to Figure 2A,
is incorporated into a breathing mask 132. The breathing mask 132 comprises a mask
body 134 designed to fit over a patient's mouth and nose when in use. A flexible strap
136 is provided to wrap around a patient's head to hold the mask body 134 in a close
relationship with the patient's face. Each side of the mask body 132 is provided with
discontinuous circular aperture 138 to allow air and other gases to flow into and
out of the mask body 132 when in use.
In the embodiment shown in Figure 7, the gas flow indicator 130 is provided in an
inlet port 140 configured to be connected to an oxygen supply through tubing 142.
Accordingly, the patient can be supplied with oxygen through the inlet port 140 and
air through the circular apertures 138. When oxygen is being supplied to the patient
through the inlet port 140, the gas flow indicator 130 will provide an audible indication
that gas is flowing. In addition, the sound generated by the gas flow indicator 130
may be interrupted by the patient<'>s breathing. Furthermore, when no oxygen is being
supplied to the patient, the patient's breathing may cause the gas flow indicator
130 to generate a sound. Accordingly, the breathing mask 132 can be configured such
that the gas flow indicator 130 generates an audible sound in response to selected
conditions.
[0036] In some embodiments, the gas flow indicator 130 may be configured so that it can
be disabled or removed by medical staff so that the device in which the gas flow indicator
130 is provided (e.g. an oxygen delivery device) can function without the gas flow
indicator function. Furthermore, the volume of the sound created by the gas flow indicator
130 may be adjustable.
It is noted that embodiments of the present invention comprise any oxygen enrichment
device having a gas flow indicator that produces a sound to indicate when oxygen is
flowing through the device. The device may be further configured such that the sound
is interrupted by a patient's breathing. Moreover, the device may be configured such
that it can be reverted or changed into a traditional oxygen enrichment device by
disabling or removing the oxygen flow indicator.
[0037] It will be appreciated by persons skilled in the art that various modifications may
be made to the above embodiments without departing from the scope of the present invention.
1. Gasatemmaske (132) einschließlich eines Flussanzeigers (130), der dazu konfiguriert
ist, eine hörbare Angabe eines Gasflusses zu liefern, wobei die Atemmaske (132) zum
Liefern von Luft oder einem Gemisch von Luft und Sauerstoff, die bzw. das durch wenigstens
einen Einlass (140) geliefert wird, an einen Patienten konfiguriert ist, wobei der
Gasflussanzeiger (130) in dem wenigstens einen Einlass (140) bereitgestellt ist und
dazu ausgelegt ist, eine hörbare Angabe zu liefern, wenn Gas korrekt in die Maske
hinein- und/oder aus dieser herausfließt, dadurch gekennzeichnet, dass der Gasflussanzeiger so ausgelegt ist, dass ein Ton, der durch diesen erzeugt wird,
durch die Atmung eines Patienten erzeugt oder unterbrochen wird.
2. Atemmaske nach Anspruch 1, wobei der Gasflussanzeiger so konfiguriert ist, dass die
Anwesenheit eines hörbaren Tons einen korrekten Gasfluss signalisiert und die Abwesenheit
eines hörbaren Tons einen inkorrekten Gasfluss signalisiert.
3. Atemmaske nach Anspruch 1, wobei der Gasflussanzeiger so konfiguriert ist, dass die
Abwesenheit eines hörbaren Tons einen korrekten Gasfluss signalisiert und die Anwesenheit
eines hörbaren Tons einen inkorrekten Gasfluss signalisiert.
4. Atemmaske nach einem vorhergehenden Anspruch, die zur Beatmung oder zum Atemwegsmanagement
konfiguriert ist.
5. Atemmaske nach einem vorhergehenden Anspruch, die nahe einem Lufteinlass von einem
Patienten angeordnet ist, so dass sie anzeigt, falls ein Problem dabei besteht, dass
die Gase zu dem Patienten gelangen.
6. Atemmaske nach einem vorhergehenden Anspruch, die als eine Einwegvorrichtung konfiguriert
ist.
7. Atemmaske nach einem vorhergehenden Anspruch, wobei der Gasflussanzeiger integral
mit der Atemmaske (132) gebildet ist.
8. Atemmaske nach einem vorhergehenden Anspruch, wobei der Gasflussanzeiger nur dazu
konfiguriert ist, einen hörbaren Ton zu liefern, wenn Gas mit einer vorbestimmten
Flussrate fließt.
1. Masque respiratoire à gaz (132) incluant un indicateur de débit (130) configuré pour
fournir une indication audible de débit de gaz, le masque respiratoire (132) étant
configuré pour fournir de l'air ou un mélange d'air et d'oxygène fourni à travers
au moins une entrée (140) à un patient, l'indicateur de débit de gaz (130) étant prévu
dans l'au moins une entrée (140) et agencé pour fournir une indication audible lorsqu'un
gaz s'écoule correctement dans le, et/ou hors du, masque, caractérisé en ce que l'indicateur de débit de gaz est agencé de telle sorte qu'un son généré par celui-ci
soit généré ou interrompu par la respiration d'un patient.
2. Masque respiratoire selon la revendication 1, dans lequel l'indicateur de débit de
gaz est configuré de telle sorte que la présence d'un son audible signale un débit
de gaz correct et l'absence d'un son audible signale un débit de gaz incorrect.
3. Masque respiratoire selon la revendication 1 dans lequel l'indicateur de débit de
gaz est configuré de telle sorte que l'absence d'un son audible signale un débit de
gaz correct et la présence d'un son audible signale un débit de gaz incorrect.
4. Masque respiratoire selon une quelconque revendication précédente, configuré pour
la gestion de soins respiratoires et/ou de voies respiratoires.
5. Masque respiratoire selon une quelconque revendication précédente, disposé près d'une
entrée d'air d'un patient afin d'indiquer s'il existe un problème avec les gaz parvenant
au patient.
6. Masque respiratoire selon une quelconque revendication précédente, configuré sous
forme de dispositif jetable.
7. Masque respiratoire selon une quelconque revendication précédente, dans lequel l'indicateur
de débit de gaz est formé de façon monobloc avec le masque respiratoire (132).
8. Masque respiratoire selon une quelconque revendication précédente, dans lequel l'indicateur
de débit de gaz est configuré seulement pour fournir un son audible lorsqu'un gaz
s'écoule à un débit prédéterminé.